vital pulp therapy to treat irreversible pulpitis
Phase 3
- Conditions
- vital pulp therapy to treat irrevesible pulpitis.
- Registration Number
- IRCT138706131191N1
- Lead Sponsor
- Iran Center of Endodontics Research center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 600
Inclusion Criteria
Diagnostic criteria:
1) Patient reports pain of endodontic origin
2) Diagnosis of irreversible pulpitis
-Eligibility criteria:
1) Molar tooth
2) Patient chooses to have tooth extraction for pain relief
3) Age 9–65 years
4) Both gender
5) The patient had read and thoroughly understood the questionnaires
6) Written informed consent
-Exclusion criteria:
1) Moderate or severe periodontitis
2) None restorable tooth
3) Internal or external root resorption
4) Root canal calcification
5) No bleeding after access cavity preparation
6) Analgesic taken within the last 4 h
7) Active systemic disease
8) The patient was pregnant or nursing
9) History of opioid addiction or abuse
10) Temporary residency
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical success of pulpotomy. Timepoint: from treatment time to 24 month after treatment. Method of measurement: clinical examination (percusion,soft tissue palpation ,observation of periapical soft tissue).;Radiographical success of pulpotomy. Timepoint: from treatment time to 24 month after treatment. Method of measurement: priapical radiography(periodental tissue health).
- Secondary Outcome Measures
Name Time Method Pain value. Timepoint: befor treatment ,6 hours after treatment ,12 hours after treatment and after that every 12 hours to 7th day. Method of measurement: Visual Analogue Scale.